Variant #0000331743 (NC_000007.13:g.100175010C>T, NM_002319.3:c.1181G>A (LRCH4))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100175010C>T
DNA change (hg38) g.100577387C>T
Published as LRCH4(NM_001289934.1):c.1181G>A (p.(Arg394Gln))
ISCN -
DB-ID LRCH4_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01241 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAP25 NM_001168682.1 -?/. - c.-3918G>A r.(?) p.(=)
LRCH4 NM_002319.3 -?/. - c.1181G>A r.(?) p.(Arg394Gln)


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